TCTN2 Gene Meckel Syndrome Type 8 Genetic Test
Test Name: TCTN2 Gene Meckel syndrome type 8 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Hepatology Nephrology Endocrinology Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for TCTN2 Gene Meckel syndrome type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN2 Gene Meckel syndrome type 8 NGS Genetic DNA Test gene TCTN2
Test Details
The TCTN2 gene is associated with Meckel syndrome type 8 (MKS8), which is a rare genetic disorder characterized by various abnormalities affecting multiple organ systems. MKS8 is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated TCTN2 gene (one from each parent) to develop the disorder.
NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Meckel syndrome type 8, NGS Genetic Testing can be used to identify mutations in the TCTN2 gene, providing a definitive diagnosis for individuals suspected of having the condition.
This type of genetic testing involves collecting a sample of DNA (usually through a blood or saliva sample) from the individual being tested. The DNA is then sequenced using NGS technology, which allows for the detection of various types of genetic alterations, such as single nucleotide variants, small insertions or deletions, and larger structural variants.
The resulting sequence data is then analyzed and compared to a reference sequence to identify any mutations in the TCTN2 gene. NGS Genetic Testing for Meckel syndrome type 8 can help confirm a clinical diagnosis, provide information about the inheritance pattern, and assist in genetic counseling and family planning.
It is important to note that this type of testing is typically ordered by a healthcare professional and should be interpreted by a qualified geneticist or genetic counselor.
| Test Name | TCTN2 Gene Meckel syndrome type 8 Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TCTN2 Gene Meckel syndrome type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN2 Gene Meckel syndrome type 8 NGS Genetic DNA Test gene TCTN2 |
| Test Details |
The TCTN2 gene is associated with Meckel syndrome type 8 (MKS8), which is a rare genetic disorder characterized by various abnormalities affecting multiple organ systems. MKS8 is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated TCTN2 gene (one from each parent) to develop the disorder. NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Meckel syndrome type 8, NGS Genetic Testing can be used to identify mutations in the TCTN2 gene, providing a definitive diagnosis for individuals suspected of having the condition. This type of genetic testing involves collecting a sample of DNA (usually through a blood or saliva sample) from the individual being tested. The DNA is then sequenced using NGS technology, which allows for the detection of various types of genetic alterations, such as single nucleotide variants, small insertions or deletions, and larger structural variants. The resulting sequence data is then analyzed and compared to a reference sequence to identify any mutations in the TCTN2 gene. NGS Genetic Testing for Meckel syndrome type 8 can help confirm a clinical diagnosis, provide information about the inheritance pattern, and assist in genetic counseling and family planning. It is important to note that this type of testing is typically ordered by a healthcare professional and should be interpreted by a qualified geneticist or genetic counselor. |
